HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 22493753, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 10633115 | HCID 10633115 | — |
| Product | HCID 22493753 | HCID 22493753 | — |
Reaction Steps
A solution of aldehyde 102 (230 mg) in diethyl ether (30 mL) is placed in a separatory funnel and treated with a solution of Preparation of 1-(1-Butyl)-2-phenyl-5-(1-[N-[{3,4-methylenedioxyphenylmethyl]}-N-[phenylmethyl]aminoethylimidazole) methyl lithium (1.4 M in THF, 1.5 ml). After 10 min. the solution is washed with ammonium chloride solution (1 M, 20 ml), dried (Na2SO4) and concentrated. The resulting dark oil is purified by preparative TLC (10% MeOH/CHCl3) to provide compound 107 as a colorless oil (180 mg). 1H NMR (400 MHz, CDCl3) δ 7.56 (d, J=2 Hz, 2H), 7.4 (m, 3H), 7.01 (s, 1H), 4.86 (q, J=7 Hz, 1H), 4.18 (m, 1H), 4.0 (m, 1H), 1.63 (d, J=6.6 Hz, 3H), 1.63 (m, 2H), 1.23 (m, 2H), 0.81 (t, J=7 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06884815B1 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-688cc37fc07b4582bfe8180799a3d035 |
| Source note | uspto-grants-2005_04 |